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rs193302991

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193302991(A;A)
Make rs193302991(A;G)
Make rs193302991(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeMT
Position15301
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs193302991
ebirs193302991
HLIrs193302991
Exacrs193302991
Varsomers193302991
Maprs193302991
PheGenIrs193302991
hapmaprs193302991
1000 genomesrs193302991
hgdprs193302991
ensemblrs193302991
gopubmedrs193302991
geneviewrs193302991
scholarrs193302991
googlers193302991
pharmgkbrs193302991
gwascentralrs193302991
openSNPrs193302991
23andMers193302991
23andMe allrs193302991
SNP Nexus

SNPshotrs193302991
SNPdbers193302991
MSV3drs193302991
GWAS Ctlgrs193302991
Max Magnitude0
ClinVar
Risk rs193302991(T;T)
Alt rs193302991(T;T)
Reference rs193302991(C;C)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene CYTB
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_012920.1:m.15301G>A
CLNSRC
CLNACC RCV000128806.1,